Page last updated: 2024-11-11

pleiocarpamine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

pleiocarpamine: corymine compound is the main indole alkaloid; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5385014
CHEMBL ID3338254
CHEBI ID141939
MeSH IDM0295830

Synonyms (16)

Synonym
pleocarpamine
pleiocarpamine
6393-66-4
nsc374523
nsc-374523
CHEBI:141939
DTXSID80419616
CHEMBL3338254
(16s,19e)-17-methoxy-17-oxo-19,20-didehydro-1,16-cyclocorynan
Q15425259
methyl (13e,14s,16s,18s)-13-ethylidene-1,11-diazapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17)-tetraene-18-carboxylate
nsc 374523
4j3pv95anl ,
unii-4j3pv95anl
2h-2,12-methanoindolo(2,3-a)quinolizine-13-carboxylic acid, 3-ethylidene-1,3,4,6,7,12b-hexahydro-, methyl ester, (2s,3e,12bs,13s)-
(+)-pleiocarpamine
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
monoterpenoid indole alkaloidA terpenoid indole alkaloid which is biosynthesised from L-tryptophan and diisoprenoid (usually secolaganin) building blocks.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID1163733Cytotoxicity against vincristine-sensitive human KB cells2014Journal of natural products, Sep-26, Volume: 77, Issue:9
Oxidized derivatives of macroline, sarpagine, and pleiocarpamine alkaloids from Alstonia angustifolia.
AID1163734Cytotoxicity against vincristine-resistant human KB/VJ300 cells2014Journal of natural products, Sep-26, Volume: 77, Issue:9
Oxidized derivatives of macroline, sarpagine, and pleiocarpamine alkaloids from Alstonia angustifolia.
AID1163735Cytotoxicity against multi-drug resistant human KB/VJ300 cells in presence of 0.1 ug/ml vincristine2014Journal of natural products, Sep-26, Volume: 77, Issue:9
Oxidized derivatives of macroline, sarpagine, and pleiocarpamine alkaloids from Alstonia angustifolia.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (11.11)18.2507
2000's0 (0.00)29.6817
2010's7 (77.78)24.3611
2020's1 (11.11)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other10 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]